Liang Linlin, Mai Ai, Zhou Jiazhen, Xu Enwu, Wang Jin, Yang Qiaoyuan
Institute of Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, Guangdong 511436, China.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Mar 10;39(3):286-292. doi: 10.3760/cma.j.cn511374-20200809-00594.
To assess the influence of rs2910164 G/C single nucleotide polymorphism (SNP) of the miR-146a gene on its expression and susceptibility to gastric cancer.
Fifty three gastric cancer patients and six gastric cancer cell lines were selected for determining the miR-146a expression by Taqman quantitative PCR. A model was constructed to assess the influence of miR-146a overexpression on the growth of AGS gastric cancer cells. A case-control study involving 417 gastric cancer patients and 420 cancer-free individuals was then conducted, and the allelic and genotypic frequencies of the rs2910164 G/C SNP were compared. The genotypes of all subjects were determined by using a Taqman allelic discrimination assay. A Taqman assay was also used to quantify mature and pri-miR-146a transcripts among 65 gastric cancer patients with known genotypes.
The expression of miR-146a was down-regulated among the 53 gastric cancer patients and six gastric cancer cell lines. Over-expression of miR-146a has suppressed the growth of gastric cancer by inhibiting the G1/S-phase transition of AGS cells. The case-control study showed that subjects with GC/CC genotypes had significantly lower risk for gastric cancer compared with those with GG genotype. In addition, miR-146a G/C SNP has significantly increased the level of mature miR-146a in those with GC/CC genotype compared with GG genotype.
Down-regulation of miR-146a may play an important role in the pathogenesis of gastric cancer. The rs2910164 polymorphism of the miR-146a gene may reduce the risk of gastric cancer by influencing the processing of mature miR-146a.
评估miR-146a基因的rs2910164 G/C单核苷酸多态性(SNP)对其表达及胃癌易感性的影响。
选取53例胃癌患者和6种胃癌细胞系,采用Taqman定量PCR法测定miR-146a的表达。构建模型评估miR-146a过表达对AGS胃癌细胞生长的影响。随后进行一项病例对照研究,纳入417例胃癌患者和420例无癌个体,比较rs2910164 G/C SNP的等位基因和基因型频率。使用Taqman等位基因鉴别分析确定所有受试者的基因型。还采用Taqman分析对65例已知基因型的胃癌患者中的成熟和初级miR-146a转录本进行定量。
53例胃癌患者和6种胃癌细胞系中miR-146a的表达下调。miR-146a的过表达通过抑制AGS细胞的G1/S期转换抑制了胃癌的生长。病例对照研究表明,与GG基因型患者相比,GC/CC基因型患者患胃癌的风险显著降低。此外,与GG基因型相比,miR-146a G/C SNP使GC/CC基因型患者的成熟miR-146a水平显著升高。
miR-146a的下调可能在胃癌发病机制中起重要作用。miR-146a基因的rs2910164多态性可能通过影响成熟miR-146a的加工过程降低胃癌风险。